Canonical Allele Identifier: CA2841438401

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.44300506G>T , CM000668.2:g.44300506G>T GRCh38
NC_000006.11:g.44268243G>T , CM000668.1:g.44268243G>T GRCh37
NC_000006.10:g.44376221G>T NCBI36
NG_031952.1:g.17821C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000244571.5:c.*41C>A (AARS2) MANE Select ENSP00000244571.4:n.*41C>A
ENST00000244571.4:c.*41C>A (AARS2) ENSP00000244571.4:n.*41C>A
ENST00000438774.2:c.577-6437G>T (TMEM151B) ENSP00000409337.2:n.577-6437G>T
ENST00000505802.1:c.314-6437G>T
NM_020745.3:c.*41C>A (AARS2) NP_065796.1:n.*41C>A
XM_005249245.2:c.*41C>A (AARS2) XP_005249302.1:n.*41C>A
XM_011514764.1:c.2793+650C>A (AARS2) XP_011513066.1:n.2793+650C>A
XM_005249245.3:c.*41C>A (AARS2) XP_005249302.1:n.*41C>A
XM_011514764.2:c.2793+650C>A (AARS2) XP_011513066.1:n.2793+650C>A
XM_017011112.1:c.*41C>A (AARS2) XP_016866601.1:n.*41C>A
NM_020745.4:c.*41C>A (AARS2) MANE Select NP_065796.2:n.*41C>A
NM_001318876.2:c.946-141384G>T (POLR1C) NP_001305805.1:n.946-141384G>T